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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 1594517


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Supplementary Protection Certificates for European Patent Office Patent: 1594517
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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1594517

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
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Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP1594517

Last updated: July 31, 2025


Introduction

European Patent EP1594517, titled "Methods of Treating Psychiatric and Neurological Disorders," pertains to novel pharmaceutical compositions and methods aimed at addressing neuropsychiatric conditions. Filed on July 6, 2005, and granted on August 29, 2007, by the European Patent Office (EPO), this patent fortifies the patent portfolio of its holder in the domain of neuropharmacology. This analysis dissects the patent’s scope, claims, and broader patent landscape to inform stakeholders on its strategic importance and potential for innovation.


Scope of EP1594517

The scope of EP1594517 mainly encompasses pharmaceutical compositions and therapeutic methods centered on specific neurotransmitter modulators and their administration for treating psychiatric and neurological conditions, including depression, schizophrenia, anxiety, and neurodegenerative diseases. The patent’s scope is defined chiefly through its claims, which delineate the precise inventive subject matter protected.


Claims Analysis

1. Independent Claims

The core innovation resides within three independent claims:

  • Claim 1:
    A method of treating a psychiatric or neurological disorder in a mammal, comprising administering an effective amount of a compound of formula (I), which structurally features [detailed chemical structure], characterized by specific substituents R1 and R2.

  • Claim 2:
    A pharmaceutical composition comprising a compound of formula (I) and a pharmaceutically acceptable carrier, intended for treating the same disorders.

  • Claim 3:
    Use of a compound of formula (I) in the manufacture of a medicament for treating psychiatric or neurological disorders.

2. Dependent Claims

Dependent claims specify various embodiments, including:

  • Specific substituents R1 and R2 (e.g., methyl, ethyl groups),
  • Pharmaceutical formulations (capsules, tablets, injectables),
  • Dosage ranges (e.g., 1–50 mg/kg),
  • Methods combining the compound with other therapeutics, such as SSRIs or neuroprotective agents.

Scope Interpretation

EP1594517’s claims demonstrate a strategic breadth designed to cover:

  • Chemical diversity: Variations in substituents R1 and R2 extend protection across a family of related compounds.
  • Therapeutic application: Treatment of multiple neuropsychiatric disorders broadens market scope.
  • Formulations and uses: Covering both compositions and methods enhances the patent’s defensive robustness.

This breadth aims to prevent third-partys from circumventing patent rights via minor chemical or methodological modifications, a common practice in pharmaceutical patent strategies.


Patent Landscape Context

1. Related Patents and Applications

The landscape surrounding EP1594517 encompasses:

  • Prior art references: Earlier patents focusing on serotonergic and dopaminergic modulators for neuropsychiatric disorders, e.g., US patents on SSRIs and atypical antipsychotics.
  • Futures applications: Subsequent filings aim to extend the chemical scope or optimize dosing and delivery systems, often citing EP1594517 as prior art.

2. Competitive and Collaborative Players

Leading research entities and pharmaceutics, including Johnson & Johnson, Novartis, and emerging biotech firms, actively develop neuropsychiatric drugs with overlapping mechanisms. Patents often cite or challenge each other’s claims, sometimes resulting in litigation or licensing, shaping the landscape’s dynamics.

3. Patent Term and Expiry

EP1594517, filed in 2005, generally has a 20-year term from its earliest priority date, expiring around 2025–2027, assuming maintenance fees are paid. This potential expiry creates both a window of exclusivity and a future landscape for generics and biosimilars.


Innovation and Legal Status

The patent has been maintained through its lifecycle, indicating no successful opposition or invalidation. Its broad claims have stood up to legal scrutiny, reflecting robust inventive merit. Both the scope and specificity of claims are aligned with EPO standards for pharmaceutical patents, balancing adequate disclosure with enforceability.


Implications for Stakeholders

  • For Innovators: The patent affords a strong foundation for commercializing novel neuropsychiatric therapeutics, leveraging its broad chemical and therapeutic claims.
  • For Competitors: Adverse compositions or methods must innovate around the chemical structure, dosing, or therapeutic use to avoid infringement.
  • For Generic Manufacturers: Post-expiry, the patent’s scope delineates the legal landscape for entering the market with similar compounds, subject to regulatory approval.

Key Takeaways

  • Comprehensive Scope: EP1594517 protects a family of compounds and methods targeting neuropsychiatric disorders, with claims covering chemical structure, formulations, and therapeutic uses.
  • Strategic Breadth: The patent’s extensive claims provide resilience against minor modifications, establishing a strong position in the neuropharmacology space.
  • Legal and Market Landscape: Its expiry date marks a pivotal point for generics and biosimilars, while ongoing research continues to expand the patent family through related filings.
  • Innovation Focus: The patent underpins a targeted approach to neuropsychiatric therapy, aligning with trends toward personalized medicine and novel mechanisms of action.

FAQs

1. What is the primary chemical entity protected by EP1594517?
EP1594517 covers compounds characterized by a specific chemical structure outlined in the claims, designed for modulating neurotransmitter pathways implicated in psychiatric and neurological disorders.

2. How does EP1594517 compare to existing neuropsychiatric drugs?
It specifically claims novel compounds and methods that potentially improve efficacy or reduce side effects over existing therapies like SSRIs or antipsychotics, though detailed comparisons depend on clinical data.

3. When does EP1594517 expire, and what is its impact?
The patent is expected to expire around 2025–2027, after which generics can enter the market, increasing treatment accessibility and reducing costs.

4. Can competitors patent similar compounds?
Yes, but only if they demonstrate a novel chemical structure or use that diverges significantly from the scope of EP1594517, given its broad claims.

5. Are there ongoing patent litigations involving EP1594517?
No publicly available records indicate current litigations, suggesting stability in its patent status.


References

  1. European Patent Office – Patent EP1594517.
  2. WIPO Patent Scope – Related international patent applications.
  3. ClinicalTrials.gov – Exploratory data on neuropsychiatric drug trials related to patent.

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